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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
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1989 1
1992 1
1994 1
1997 1
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1999 1
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2003 3
2004 1
2005 1
2014 1
2015 2
2016 2
2018 2
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2020 1
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2023 4
2024 1

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28 results

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Page 1
Overview of primary adult retroperitoneal tumours.
Improta L, Tzanis D, Bouhadiba T, Abdelhafidh K, Bonvalot S. Improta L, et al. Eur J Surg Oncol. 2020 Sep;46(9):1573-1579. doi: 10.1016/j.ejso.2020.04.054. Epub 2020 May 21. Eur J Surg Oncol. 2020. PMID: 32600897 Review.
According to the World Health Organization (WHO) classification of tumours, mesenchymal benign and malignant tumours (including sarcomas and, currently, neurogenic tumours), parasympathetic tumours, extragonadal germ cell tumours, and lymphoid tumours have been identified. …
According to the World Health Organization (WHO) classification of tumours, mesenchymal benign and malignant tumours (including sarco …
Intradural spinal tumors in adults-update on management and outcome.
Ottenhausen M, Ntoulias G, Bodhinayake I, Ruppert FH, Schreiber S, Förschler A, Boockvar JA, Jödicke A. Ottenhausen M, et al. Neurosurg Rev. 2019 Jun;42(2):371-388. doi: 10.1007/s10143-018-0957-x. Epub 2018 Feb 17. Neurosurg Rev. 2019. PMID: 29455369 Review.
Technical advances in imaging, neuromonitoring, minimally invasive approaches, and radiotherapy have improved the outcome of intradural spinal tumors. However, the outcome in malignant intramedullary tumors remains poor. While surgery is the mainstay treatment for many of …
Technical advances in imaging, neuromonitoring, minimally invasive approaches, and radiotherapy have improved the outcome of intradural spin …
The many faces of solitary fibrous tumor; diversity of histological features, differential diagnosis and role of molecular studies and surrogate markers in avoiding misdiagnosis and predicting the behavior.
Tariq MU, Din NU, Abdul-Ghafar J, Park YK. Tariq MU, et al. Diagn Pathol. 2021 Apr 20;16(1):32. doi: 10.1186/s13000-021-01095-2. Diagn Pathol. 2021. PMID: 33879215 Free PMC article. Review.
MAIN BODY: Apart from diversity in morphological features seen even in conventional SFT, two histologic variants (fat-forming and giant cell-rich) are also recognized. In addition, a malignant form and dedifferentiation are well recognized. Owing to diverse histological fe …
MAIN BODY: Apart from diversity in morphological features seen even in conventional SFT, two histologic variants (fat-forming and giant cell …
Management of Central and Peripheral Nervous System Tumors in Patients with Neurofibromatosis.
Brown R. Brown R. Curr Oncol Rep. 2023 Dec;25(12):1409-1417. doi: 10.1007/s11912-023-01451-z. Epub 2023 Oct 31. Curr Oncol Rep. 2023. PMID: 37906356 Review.
RECENT FINDINGS: Mek inhibitors have provided a much-needed therapeutic avenue for NF1 patients with unresectable plexiform neurofibromas (PN), both for reduction of tumor bulk and for improvement in symptoms. ...This article provides an update regarding considerations and …
RECENT FINDINGS: Mek inhibitors have provided a much-needed therapeutic avenue for NF1 patients with unresectable plexiform neurofibr …
Diagnosis, classification, and management of soft tissue sarcomas.
Mankin HJ, Hornicek FJ. Mankin HJ, et al. Cancer Control. 2005 Jan-Feb;12(1):5-21. doi: 10.1177/107327480501200102. Cancer Control. 2005. PMID: 15668648 Free article. Review.
Advances in imaging, as well as improvements in surgical techniques and adjunctive treatment methods, have improved care for patients with these unusual disorders. METHODS: The various types of soft tissue tumors are defined, and the statistics for the Orthopaedic Oncology …
Advances in imaging, as well as improvements in surgical techniques and adjunctive treatment methods, have improved care for patients …
Gastrointestinal stromal tumors (GISTs): definition, occurrence, pathology, differential diagnosis and molecular genetics.
Miettinen M, Lasota J. Miettinen M, et al. Pol J Pathol. 2003;54(1):3-24. Pol J Pathol. 2003. PMID: 12817876 Review.
GISTs are the most common mesenchymal neoplasms of the GI tract, and encompass most tumors previously classified as gastric and intestinal smooth muscle tumors. GISTs typically present in adults over 40 years (median age 55-60 years) and only exceptionally in children. ... …
GISTs are the most common mesenchymal neoplasms of the GI tract, and encompass most tumors previously classified as gastric and intestinal s …
Malignant Peripheral Nerve Sheath Tumors of the Brachial Plexus: A Single-Center Experience on Diagnosis, Management, and Outcomes.
Donaldson EK, Winter JM, Chandler RM, Clark TA, Giuffre JL. Donaldson EK, et al. Ann Plast Surg. 2023 Apr 1;90(4):339-342. doi: 10.1097/SAP.0000000000003462. Epub 2023 Feb 4. Ann Plast Surg. 2023. PMID: 36752552 Review.
Malignant peripheral nerve sheath tumors are aggressive tumors with high rates of local recurrence and metastasis. ...All patients were referred to oncology and received radiation therapy. CONCLUSIONS: Malignant peripheral nerve sheath tumors must be suspecte …
Malignant peripheral nerve sheath tumors are aggressive tumors with high rates of local recurrence and metastasis. ...All patients we …
Rare benign liver tumors that require differentiation from hepatocellular carcinoma: focus on diagnosis and treatment.
Luo L, Wang T, Cheng M, Ge X, Song S, Zhu G, Xiao Y, Deng W, Xie J, Shan R. Luo L, et al. J Cancer Res Clin Oncol. 2023 Jul;149(7):2843-2854. doi: 10.1007/s00432-022-04169-w. Epub 2022 Jul 5. J Cancer Res Clin Oncol. 2023. PMID: 35789428
It is difficult to determine the nature of partial rare BLTs and not easy to distinguish from malignant liver tumors. This study aimed to analysis clinical features, diagnosis and treatment of rare BLTs to reduce misdiagnosis and provide reference for clinical practice. ME …
It is difficult to determine the nature of partial rare BLTs and not easy to distinguish from malignant liver tumors. This study aime …
Management and prognosis of malignant peripheral nerve sheath tumors: The experience of the French Sarcoma Group (GSF-GETO).
Valentin T, Le Cesne A, Ray-Coquard I, Italiano A, Decanter G, Bompas E, Isambert N, Thariat J, Linassier C, Bertucci F, Bay JO, Bellesoeur A, Penel N, Le Guellec S, Filleron T, Chevreau C. Valentin T, et al. Eur J Cancer. 2016 Mar;56:77-84. doi: 10.1016/j.ejca.2015.12.015. Epub 2016 Jan 26. Eur J Cancer. 2016. PMID: 26824706
BACKGROUND: Malignant peripheral nerve sheath tumors (MPNST) are a rare subtype of soft tissue sarcoma. ...An unsolved issue is whether NF1-related and sporadic forms of MPNST have a different prognosis, and should be managed differently. MATERIAL AND METHODS: Adult …
BACKGROUND: Malignant peripheral nerve sheath tumors (MPNST) are a rare subtype of soft tissue sarcoma. ...An unsolved issue is wheth …
Surgical management of malignant melanotic nerve sheath tumors: an institutional experience and systematic review of the literature.
Ghaith AK, Johnson SE, El-Hajj VG, Akinduro OO, Ghanem M, De Biase G, Michaelides L, Bon Nieves A, Marsh WR, Currier BL, Atkinson JL, Spinner RJ, Bydon M. Ghaith AK, et al. J Neurosurg Spine. 2023 Oct 20;40(1):28-37. doi: 10.3171/2023.8.SPINE23427. Print 2024 Jan 1. J Neurosurg Spine. 2023. PMID: 37862711
OBJECTIVE: Malignant melanotic nerve sheath tumors are rare tumors characterized by neoplastic melanin-producing Schwann cells. ...Most patients underwent gross-total resection (GTR) (n = 41, 66.1%), followed by subtotal resection (STR) (n = 12, 19.4%), STR with radiation …
OBJECTIVE: Malignant melanotic nerve sheath tumors are rare tumors characterized by neoplastic melanin-producing Schwann cells. ...Mo …
28 results